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Craniofacial Dysostosis

Known as: Crouzon disease, syndrome crouzon's, crouzon's syndrome 
A syndrome inherited in an autosomal dominant pattern. It is characterized by early fusion of the bones of the skull and face. Patients have a… Expand
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2008
Highly Cited
2008
We have analysed the contributions of neural crest and mesoderm to mammalian craniofacial mesenchyme and its derivatives by cell… Expand
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Review
2004
Review
2004
Airway management for patients with craniofacial disorders poses many challenges. The anaesthesiologist must be familiar with the… Expand
Review
2001
Review
2001
&NA; The nascent field of craniofacial distraction osteogenesis has not yet been subjected to a rigorous evaluation of techniques… Expand
Highly Cited
2000
Highly Cited
2000
Fibroblast growth factors (FGF) play a critical role in bone growth and development affecting both chondrogenesis and… Expand
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Highly Cited
1995
Highly Cited
1995
Apert syndrome is a distinctive human malformation comprising craniosynostosis and severe syndactyly of the hands and feet. We… Expand
Highly Cited
1995
Highly Cited
1995
The anterior part of the vertebrate head expresses a group of homeo box genes in segmentally restricted patterns during… Expand
Highly Cited
1994
Highly Cited
1994
Jackson-Weiss syndrome is an autosomal dominant condition characterized by craniosynostosis, foot anomalies and great phenotypic… Expand
Review
1988
Review
1988
  • D. Noden
  • Development
  • 1988
  • Corpus ID: 7803765
Craniofacial mesenchyme is composed of three mesodermal populations - prechordal plate, lateral mesoderm and paraxial mesoderm… Expand
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Review
1988
Review
1988
Environmental agents including ethanol, 13-cis retinoic acid (RA, Accutane), the antimetabolite methotrexate, periods of hypoxia… Expand
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